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一种使用超生物素化寡核苷酸探针的快速比色原位mRNA杂交技术,用于分析小鼠结肠癌细胞中的mdr1。

A rapid colorimetric in situ mRNA hybridization technique using hyperbiotinylated oligonucleotide probes for analysis of mdr1 in mouse colon carcinoma cells.

作者信息

Bucana C D, Radinsky R, Dong Z, Sanchez R, Brigati D J, Fidler I J

机构信息

Department of Cell Biology, University of Texas M.D. Anderson Cancer Center, Houston 77030.

出版信息

J Histochem Cytochem. 1993 Apr;41(4):499-506. doi: 10.1177/41.4.8095509.

Abstract

We describe the development of a rapid colorimetric in situ hybridization technique utilizing oligonucleotide probes labeled with six biotin molecules at the 3' end to detect mdr1 in mouse colon cancer cells growing in culture and in vivo. mRNA integrity was verified by the use of a multibiotinylated poly d(T) oligonucleotide, and the specificity of the reaction was confirmed by use of labeled sense and anti-sense probes in serial cryostat sections and cultured cells. The multiple biotin label produced a strong signal after a short hybridization time. Avidin-alkaline phosphatase detection and the capillary technology used in the Microprobe Accelerated System allowed completion of the procedure in less than 5 hr. Excellent correlations with the MDR phenotype of the cells, Northern blot analysis, and immunohistochemistry recommend this procedure for identifying cells that express the MDR phenotype in culture and in vivo.

摘要

我们描述了一种快速比色原位杂交技术的开发,该技术利用在3'端标记有六个生物素分子的寡核苷酸探针来检测培养中和体内生长的小鼠结肠癌细胞中的mdr1。通过使用多生物素化的聚d(T)寡核苷酸验证mRNA完整性,并通过在连续冷冻切片和培养细胞中使用标记的正义和反义探针来确认反应的特异性。多个生物素标记在短杂交时间后产生强信号。抗生物素蛋白-碱性磷酸酶检测以及微探针加速系统中使用的毛细管技术使该过程在不到5小时内完成。与细胞的MDR表型、Northern印迹分析和免疫组织化学的良好相关性推荐该方法用于鉴定培养中和体内表达MDR表型的细胞。

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